510(k) · Cleared
ClearedNature's Cradle (TM)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Infant Advantage, Inc. · FMS Bed, Pediatric Open Hospital
Cleared on Mar 22, 1991 after a 338-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.
- Decided
- Mar 22, 1991
- Review
- 338 days
- Class
- Class II
- Product code
- FMS
- Recalls
- None
- Predicates
- 0
2 later devices descend from it, 2 citing it directly.
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K901763 | Nature's Cradle (TM) | Infant Advantage, Inc. | 1991 | — |
| +1 | K960747 | Nature's Cradle Model C1500 | Infant Advantage, Inc. | 1996 | — |
| +1 | K970334 | Nature's Cradle | Infant Advantage, Inc. | 1997 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 1 | 0 |
| 1997 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in FMS? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (2)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K960747 (Infant Advantage, Inc., 1996) has gone furthest, with 1 descendant of its own.
How does its category compare?
All FMS devicesFMS Bed, Pediatric Open Hospital: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · FMS
FDA has decided no FMS device since 2007.
Median 510(k) review, days · FMS
Too few FMS 510(k)s in any year since 2007 to give a median.
Recalls per year · FMS
1in 2019
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FMS
25in 2025
MAUDE reports naming product code FMS, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 7 |
| 2008 | 0 | — | 0 | 2 |
| 2009 | 0 | — | 0 | 7 |
| 2010 | 0 | — | 0 | 20 |
| 2011 | 0 | — | 0 | 67 |
| 2012 | 0 | — | 0 | 80 |
| 2013 | 0 | — | 0 | 136 |
| 2014 | 0 | — | 0 | 157 |
| 2015 | 0 | — | 0 | 175 |
| 2016 | 0 | — | 0 | 137 |
| 2017 | 0 | — | 0 | 121 |
| 2018 | 0 | — | 0 | 113 |
| 2019 | 0 | — | 1 | 30 |
| 2020 | 0 | — | 0 | 28 |
| 2021 | 0 | — | 0 | 28 |
| 2022 | 0 | — | 0 | 22 |
| 2023 | 0 | — | 0 | 29 |
| 2024 | 0 | — | 0 | 30 |
| 2025 | 0 | — | 0 | 25 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K901763 · printed Nov 6, 2026
Cite this page
510(k) Report. “K901763: Nature's Cradle (TM).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K901763
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026